Division of Glycoscience, School of Biotechnology, Royal Institute of Technology, AlbaNova University Centre, Stockholm, Sweden.
PLoS Pathog. 2010 Aug 26;6(8):e1001070. doi: 10.1371/journal.ppat.1001070.
Oomycetes represent some of the most devastating plant and animal pathogens. Typical examples are Phytophthora infestans, which causes potato and tomato late blight, and Saprolegnia parasitica, responsible for fish diseases. Despite the economical and environmental importance of oomycete diseases, their control is difficult, particularly in the aquaculture industry. Carbohydrate synthases are vital for hyphal growth and represent interesting targets for tackling the pathogens. The existence of 2 different chitin synthase genes (SmChs1 and SmChs2) in Saprolegnia monoica was demonstrated using bioinformatics and molecular biology approaches. The function of SmCHS2 was unequivocally demonstrated by showing its catalytic activity in vitro after expression in Pichia pastoris. The recombinant SmCHS1 protein did not exhibit any activity in vitro, suggesting that it requires other partners or effectors to be active, or that it is involved in a different process than chitin biosynthesis. Both proteins contained N-terminal Microtubule Interacting and Trafficking domains, which have never been reported in any other known carbohydrate synthases. These domains are involved in protein recycling by endocytosis. Enzyme kinetics revealed that Saprolegnia chitin synthases are competitively inhibited by nikkomycin Z and quantitative PCR showed that their expression is higher in presence of the inhibitor. The use of nikkomycin Z combined with microscopy showed that chitin synthases are active essentially at the hyphal tips, which burst in the presence of the inhibitor, leading to cell death. S. parasitica was more sensitive to nikkomycin Z than S. monoica. In conclusion, chitin synthases with species-specific characteristics are involved in tip growth in Saprolegnia species and chitin is vital for the micro-organisms despite its very low abundance in the cell walls. Chitin is most likely synthesized transiently at the apex of the cells before cellulose, the major cell wall component in oomycetes. Our results provide important fundamental information on cell wall biogenesis in economically important species, and demonstrate the potential of targeting oomycete chitin synthases for disease control.
卵菌是一些最具破坏性的植物和动物病原体。典型的例子是致病疫霉,它会导致马铃薯和番茄晚疫病,以及寄生腐霉,它会导致鱼类疾病。尽管卵菌病具有经济和环境重要性,但它们的控制很困难,特别是在水产养殖业中。碳水化合物合酶对于菌丝生长至关重要,是应对病原体的有趣目标。通过生物信息学和分子生物学方法,证明了单性寄生腐霉中有 2 种不同的几丁质合酶基因(SmChs1 和 SmChs2)的存在。通过在巴斯德毕赤酵母中表达后在体外显示其催化活性,明确证明了 SmCHS2 的功能。重组 SmCHS1 蛋白在体外没有表现出任何活性,这表明它需要其他伴侣或效应物才能发挥活性,或者它参与了不同于几丁质生物合成的过程。这两种蛋白都含有微管相互作用和运输结构域,这在任何其他已知的碳水化合物合酶中都从未报道过。这些结构域参与通过胞吞作用进行的蛋白质回收。酶动力学表明,寄生腐霉几丁质合酶受到 nikkomycin Z 的竞争性抑制,定量 PCR 显示,在抑制剂存在下,它们的表达更高。将 nikkomycin Z 与显微镜结合使用表明,几丁质合酶主要在菌丝尖端活跃,在抑制剂存在下,菌丝尖端爆裂,导致细胞死亡。寄生腐霉比单性寄生腐霉对 nikkomycin Z 更敏感。总之,具有物种特异性特征的几丁质合酶参与寄生腐霉物种的尖端生长,尽管几丁质在细胞壁中的丰度非常低,但它对微生物至关重要。几丁质很可能在细胞纤维素之前在细胞的顶点短暂合成,纤维素是卵菌中主要的细胞壁成分。我们的研究结果为经济上重要的物种的细胞壁生物发生提供了重要的基础信息,并证明了针对卵菌几丁质合酶进行疾病控制的潜力。